. . . . . . . . . . . . "[These patients and others reported as FATCO seem to belong to the phenotype 'fibular aplasia with ectrodactyly.' Genetic screening for CNVs and mutations in the TP63 and WNT10B genes did not show any genetic abnormalities.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en . . . . . "2015-02-27"^^ . . "Gene-disease associations inferred from text-mining the literature."@en . "DisGeNET evidence - LITERATURE"@en . "2015-08-25T14:45:44+02:00"^^ . . . . . . . . . . . "v3.0.0.0" . "v3.0.0" .